Chemical shielding tensor and 13C–14N dipolar splitting in single crystals of L-alanine

Publisher Website
Google Scholar
Abstract
Chemical shielding tensors have been determined for three chemically distinct carbons in a single crystal of L‐alanine using proton‐enhanced 13C NMR. The results indicate that the most shielded direction is perpendicular to the s p 2 plane for the carboxyl carbon and the C 3 axis for the methyl carbon.13C–14N dipolar splittings have been observed for the Cacarbon, causing further complication in spectral analysis. Since the 14N quadrupole coupling constant is of comparable order with the 14N Zeeman interaction, 14N quadrupole interaction is effective in the 13C–14N dipolar splittings. The 14N quadrupole effect is observed and demonstrated by calculation and the sign of the quadrupole coupling constant e 2 Q q has been determined to be positive. The chemical shielding tensor for the Cacarbon is determined by considering the 13C–14N dipolar interaction and the 14N quadrupole interaction. It is shown that the 14N quadrupole interaction causes the asymmetric doublet pattern in the 13C NMR signal for the Cacarbon in magic angle spinning (MAS) experiments.

This publication has 21 references indexed in Scilit: